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ENT TREATMENT UNITS

K822252 Class I Traditional
Decision Date
1982-11-22
Sponsor / Applicant
Kelleher Corp.

Technical Specification

510(k) Submission ID K822252
Product Code ETF
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.5300
Decision Date 1982-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENT TREATMENT UNITS received FDA 510(k) clearance under submission number K822252, sponsored by Kelleher Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1982-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code ETF and 21 CFR 874.5300, within the Ear, Nose, Throat review panel as a Class I device.